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Stellate Ganglion Block

Left Sided Stellate Ganglion Blocks Impact on the Rate of Post-operative Atrial Fibrillation in Patients Undergoing Thoracic Surgery: A Pilot Study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06271707
Enrollment
48
Registered
2024-02-22
Start date
2025-05-19
Completion date
2027-07-15
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophagectomy, Pneumonectomy, Lobectomy

Keywords

Esophagectomy, Pneumonectomy, Lobectomy, Stellate Ganglion Block

Brief summary

The purpose of this study is to determine if the addition of an ultrasound guided left sided stellate ganglion block with bupivacaine in patients undergoing esophagectomy, pneumonectomy, or lobectomy will result in lower rates of postoperative atrial fibrillation as compared to standard of care.

Interventions

an ultrasound guided left stellate ganglion block with 5 mL of 0.5% bupivacaine

OTHERSaline

an ultrasound guided left stellate ganglion block with 5 mL of saline

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

This is a double blind randomized prospective controlled trial. Randomization will be 1:1.

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing esophagectomy, pneumonectomy, or lobectomy aged 18-85.

Exclusion criteria

* Patients who have an exclusion to regional anesthesia. * Patients who have exclusion to stellate blockade. * Patients who are pregnant assessed via self-report or pregnancy test if they have taken one

Design outcomes

Primary

MeasureTime frameDescription
an ultrasound guided left stellate ganglion block with 5 mL of saline.168 hours after surgeryIncidence of Atrial fibrillation in the first 168 hours after surgery.
Atrial fibrillation; Other arrhythmias; Adverse events.168 hours after surgeryAtrial fibrillation in first 24, 48, 72, 96, 120, and 144 hours; Other arrhythmias in first 24, 48, 72, 96, 120, 144 and 168 hours; Adverse events.

Countries

United States

Contacts

Primary ContactCandace Nelson
nelso377@umn.edu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026